Label: WEAKNESS- iridium pellet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated January 8, 2019

If you are a consumer or patient please visit this version.

View All Sections
  • Indications

    Indications: To be used for acute self-limiting conditions according to standard homeopathic indications

  • Active Ingredient

    IRIDIUM METALLICUM

  • Directions

    Take at onset of symptoms.  Repeat every 2 hours or as needed until relieved.  If condition persists or worsens discontinue use and consult a practitioner.

    Adults: dissolve 5-10 pellets in 1 oz. of filtered water or take dry by mouth.  Children and infants: 1-5 pellets.

  • Keep Out of Reach of Children

    Keep these and all medications out of the reach of children.

  • Warning

    If pregnant or nursing, consult a practitioner before using.

  • Inactive Ingredients

    Inactive Ingredients - Lactose, Sucrose

  • Purpose

    Purpose: WEAKNESS

  • Package Label

    Est. No. 1724217

    Natural Health Supply

    505-474-9175

    Homeopathic Medicated Pellets

    Do not use if clear bottle seal is broken. Do not use if perforated cap seal is broken.

    IRIDIUM METALLICUM 30CC

    Lot #__________________

    WEAKNESS LABEL

    res

  • INGREDIENTS AND APPEARANCE
    WEAKNESS 
    iridium pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64117-240
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IRIDIUM (UNII: 44448S9773) (IRIDIUM - UNII:44448S9773) IRIDIUM30 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    SUCROSE (UNII: C151H8M554)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64117-240-011.875 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/04/1998
    2NDC:64117-240-027.5 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/04/1998
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/04/1998
    Labeler - Natural Health Supply (018504618)
    Registrant - Natural Health Supply (018504618)
    Establishment
    NameAddressID/FEIBusiness Operations
    Natural Health Supply018504618manufacture(64117-240)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!